Abstract

BackgroundWe report here a new type of protein chip to detect antibodies in sera. This chip method was used to a prototype created to detect hepatocellular carcinoma (HCC) -related autoantibodies in the sera of hepatitis C virus (HCV) infected individuals.ResultsFive cysteine-tagged (Cys-tag) and green fluorescent protein (GFP)-fused recombinant heat shock protein 70 (HSP70), superoxide dismutase 2 (SOD2), and peroxiredoxin 6 (PRDX6), were spotted and immobilized on maleimide-incorporated diamond-like carbon (DLC) substrates. The antibodies in diluted sera were trapped by these proteins at each spot on the chip, and visualized by a fluorescence-conjugated anti-human IgG. The total immobilized protein level of each spot was detected with anti-GFP mouse IgG and a fluorescence-conjugated secondary anti-mouse IgG. The ratio between the two fluorescence intensities was used to quantify autoantibody levels in each serum sample. Heat treatment of the chip in a solution of denaturing and reducing agents, before serum-incubation, improved autoantibody detection. We tested serum samples from healthy individuals and HCC patients using the chips. The HSP70 autoantibodies were found at high levels in sera from HCV-positive HCC patients, but not in HCV-negative sera.ConclusionThis protein chip system may have useful properties to capture a specific set of antibodies for predicting the onset of particular cancers such as HCC in HCV-infected individuals.

Highlights

  • We report here a new type of protein chip to detect antibodies in sera

  • Fabrication of antigenic protein array chips Recombinant antigenic proteins of heat shock protein 70 (HSP70), superoxide dismutase 2 (SOD2) and peroxiredoxin 6 (PRDX6) were produced in E. coli BL21 strain

  • The expression of recombinant green fluorescent protein (GFP)-tagged antigenic proteins were confirmed by SDS-PAGE after purification using Ni-affinity gel (Figure 2A)

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Summary

Introduction

We report here a new type of protein chip to detect antibodies in sera. This chip method was used to a prototype created to detect hepatocellular carcinoma (HCC) -related autoantibodies in the sera of hepatitis C virus (HCV) infected individuals. Combination of information from multiple autoantibodies possibly increases the HCC detection sensitivity and specificity. Such kind of diagnostic parallel detection has been attempted using several assay systems, including polystyrene microarrays, slot blot on nitrocellulose membranes, and microarrays on sol-gel derived materials [19,20,21]

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